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La maladie de Cowden et le gène PTEN : un exemple d'intégration réussie entre clinique et biologie

Other title
Cowden disease and the PTEN gene: a successfully clinical and biological combined approach (en)
Author
LONGY, Michel1
[1] Laboratoire de génétique moléculaire, Institut Bergonié, 229, cours de l'Argonne, 33076 Bordeaux, France
Source

Bulletin du cancer. 2001, Vol 88, Num 12, pp 1153-1158 ; ref : 28 ref

CODEN
BUCABS
ISSN
0007-4551
Scientific domain
Medical oncology
Publisher
Libbey-Eurotext, Montrouge
Publication country
France
Document type
Article
Language
French
Keyword (fr)
1-Phosphatidylinositol 3-kinase Carcinogenèse Cowden syndrome Diagnostic Gène suppresseur tumeur Homme Mutation Gène PTEN Enzyme Génétique Hamartome Maladie héréditaire Peau pathologie Transferases Tumeur maligne
Keyword (en)
1-Phosphatidylinositol 3-kinase Carcinogenesis Cowden syndrome Diagnosis Tumor suppressor gene Human Mutation Enzyme Genetics Hamartoma Genetic disease Skin disease Transferases Malignant tumor
Keyword (es)
1-Phosphatidylinositol 3-kinase Carcinogénesis Cowden síndrome Diagnóstico Gen supresor tumor Hombre Mutación Enzima Genética Hamartoma Enfermedad hereditaria Piel patología Transferases Tumor maligno
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08B Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue

Discipline
Dermatology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13383916

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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